E-LIB Suche - Ergebnisse für: Costain, G.

1

MICRORNAS AND GENETIC RISK FOR TETRALOGY OF FALLOT:

Bassett, A.S. ; Costain, G.A. ; Marshall, C.R....
Canadian Journal of Cardiology. 31 (2015) 10 - p. S189-S190 , 2015

Link: https://doi.org/10.1016/..

2

Pathogenic rare copy number variants in community-based sch..:

Costain, G. ; Lionel, A. C. ; Merico, D....
Human Molecular Genetics. 22 (2013) 22 - p. 4485-4501 , 2013

Link: https://doi.org/10.1093/..

3

Individualizing Recurrence Risks for Severe Mental Illness:..:

Costain, G. ; Bassett, A. S.
Schizophrenia Bulletin. 40 (2013) 1 - p. 21-23 , 2013

Link: https://doi.org/10.1093/..

4

Perceived burden and neuropsychiatric morbidities in adults..:

Karas, D. J. ; Costain, G. ; Chow, E. W. C..
Journal of Intellectual Disability Research. 58 (2012) 2 - p. 198-210 , 2012

Link: https://doi.org/10.1111/..

5

Caregiver and adult patient perspectives on the importance ..:

Costain, G. ; Chow, E. W. C. ; Ray, P. N..
Journal of Intellectual Disability Research. 56 (2011) 6 - p. 641-651 , 2011

Link: https://doi.org/10.1111/..

6

Organs:

Costain, G. A.
Theology. 67 (1964) 530 - p. 358-359 , 1964

Link: https://doi.org/10.1177/..

7

Variant-specific changes in RAC3 function disrupt corticoge..:

Scala, M ; Nishikawa, M ; Ito, H...
issn:0006-8950. , 2022

Link: http://hdl.handle.net/11..

8

ATP1A2- and ATP1A3-associated early profound epileptic ence..:

Vetro, A ; Nielsen, HN ; Holm, R...
issn:0006-8950. , 2021

Link: http://hdl.handle.net/11..

9

Genetic contributors to risk of schizophrenia in the presen..:

Cleynen I ; Engchuan W ; Hestand M. S...
info:eu-repo/semantics/altIdentifier/pmid/32015465. , 2020

Link: http://hdl.handle.net/11..

10

Cell-based analysis of CAD variants identifies individuals ..:

Del Caño-Ochoa, F ; Ng, BG ; Abedalthagafi, M...
https://discovery.ucl.ac.uk/id/eprint/10102264/1/s41436-020-0833-2.pdf. , 2020

Link: https://discovery.ucl.ac..

11

Expanding Clinical Presentations Due to Variations in THOC2..:

Kumar, R ; Palmer, E ; Gardner, AE...
Kumar , R , Palmer , E , Gardner , AE , Carroll , R , Banka , S , Abdelhadi , O , Donnai , D , Elgersma , Y , Curry , CJ , Gardham , A , Suri , M , Malla , R , Brady , LI , Tarnopolsky , M , Azmanov , DN , Atkinson , V , Black , M , Baynam , G , Dreyer , L , Hayeems , RZ , Marshall , CR , Costain , G , Wessels , MW , Baptista , J , Drummond , J , Leffler , M , Field , M & Gecz , J 2020 , ' Expanding Clinical Presentations Due to Variations in THOC2 mRNA Nuclear Export Factor ' , Frontiers in Molecular Neuroscience , vol. 13 , 12 . https://doi.org/10.3389/fnmol.2020.00012. , 2020

Link: https://pure.eur.nl/en/p..

12

Histone H3.3 beyond cancer: Germline mutations in Histone 3..:

Bryant, L ; Li, D ; Cox, S.G...
info:eu-repo/semantics/altIdentifier/doi/10.1126/sciadv.abc9207. , 2020

Link: https://push-zb.helmholt..

13

Cell-based analysis of CAD variants identifies individuals ..:

Del Caño-Ochoa, F ; Ng, BG ; Abedalthagafi, M...
https://openaccess.sgul.ac.uk/id/eprint/112027/1/s41436-020-0833-2.pdf. , 2020

Link: https://openaccess.sgul...

14

Histone H3.3 beyond cancer: Germline mutations in Histone 3..:

Bryant L ; Li D ; Cox S. G...
info:eu-repo/semantics/altIdentifier/pmid/33268356. , 2020

Link: http://hdl.handle.net/23..

15

Parental Origin of Interstitial Duplications at 15q11.2-q13..:

Isles, AR ; Ingason, A ; Lowther, C...
https://discovery.ucl.ac.uk/id/eprint/1494709/1/Sisodiya_Parental%20Origin%20of%20Interstitial%20Duplications%20at%2015q11.2-q13.3%20in%20Schizophrenia%20and%20Neurodevelopmental%20Disorders.pdf. , 2016

Link: https://discovery.ucl.ac..